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rs863225238

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225238(C;T)
Make rs863225238(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93797456
GeneTMEM67
is asnp
is mentioned by
dbSNPrs863225238
ebirs863225238
HLIrs863225238
Exacrs863225238
Varsomers863225238
Maprs863225238
PheGenIrs863225238
hapmaprs863225238
1000 genomesrs863225238
hgdprs863225238
ensemblrs863225238
gopubmedrs863225238
geneviewrs863225238
scholarrs863225238
googlers863225238
pharmgkbrs863225238
gwascentralrs863225238
openSNPrs863225238
23andMers863225238
23andMe allrs863225238
SNP Nexus

SNPshotrs863225238
SNPdbers863225238
MSV3drs863225238
GWAS Ctlgrs863225238
Max Magnitude0
ClinVar
Risk rs863225238(T;T)
Alt rs863225238(T;T)
Reference rs863225238(C;C)
Significance Probable-Pathogenic
Disease Joubert syndrome 6
Variation info
Gene TMEM67
CLNDBN Joubert syndrome 6
Reversed 0
HGVS NC_000008.10:g.94809684C>T
CLNSRC
CLNACC RCV000201654.1,